Kii Fios First Entry Access Systems (UDI 00607915119874)
Manufactured by Applied Medical Resources Corporation
Device Regulatory Overview
The Kii Fios First Entry Access Systems (Model/Catalog Number: CFF33) is a medical device manufactured by Applied Medical Resources Corporation. This product is indexed under FDA Product Code / Category Classification K01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CFF33
- Product Code / EMDN
- K01010105
- Device Name
- Kii® Fios® Access System, Advanced Fixation
- Database Sync Date
- 2026-08-09 16:51:31
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Kii Fios First Entry Access Systems?
The registered manufacturer of record for Kii Fios First Entry Access Systems is Applied Medical Resources Corporation.
What is the Primary UDI-DI identifier for Kii Fios First Entry Access Systems?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00607915119874.
What classification code is assigned to this device?
This device is registered under product classification code K01010105.
Similar Classification Devices (K01010105)
Other Devices by Applied Medical Resources Corporation
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